WO2001011965A1 - Fongicides - Google Patents

Fongicides Download PDF

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Publication number
WO2001011965A1
WO2001011965A1 PCT/EP2000/008143 EP0008143W WO0111965A1 WO 2001011965 A1 WO2001011965 A1 WO 2001011965A1 EP 0008143 W EP0008143 W EP 0008143W WO 0111965 A1 WO0111965 A1 WO 0111965A1
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WO
WIPO (PCT)
Prior art keywords
alkyl
substituted
optionally substituted
phenyl
nhc
Prior art date
Application number
PCT/EP2000/008143
Other languages
English (en)
Inventor
Tracey Cooke
David Hardy
Brian Moloney
Peter Stanley Thomas
Chris Richard Steele
Geoffrey Gower Briggs
Original Assignee
Aventis Cropscience Gmbh
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from GBGB9919499.5A external-priority patent/GB9919499D0/en
Priority claimed from GBGB9919500.0A external-priority patent/GB9919500D0/en
Application filed by Aventis Cropscience Gmbh filed Critical Aventis Cropscience Gmbh
Priority to JP2001516328A priority Critical patent/JP4936623B2/ja
Priority to AT00960499T priority patent/ATE270817T1/de
Priority to MXPA02001453A priority patent/MXPA02001453A/es
Priority to BR0013371-0A priority patent/BR0013371A/pt
Priority to US10/049,976 priority patent/US6821992B1/en
Priority to DE60012188T priority patent/DE60012188T2/de
Priority to AU72785/00A priority patent/AU7278500A/en
Priority to EP00960499A priority patent/EP1204323B1/fr
Publication of WO2001011965A1 publication Critical patent/WO2001011965A1/fr

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
    • A01N47/30—Derivatives containing the group >N—CO—N aryl or >N—CS—N—aryl
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/61—Halogen atoms or nitro radicals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links

Definitions

  • This invention relates to compounds having fungicidal activity.
  • the invention provides the use of a compound of general formula I, complexes and salts thereof as phytopathogenic fungicides
  • a ⁇ is 2-pyridyl or its N-oxide, each of which may be substituted by up to four groups at least one of which is haloalkyl;
  • Y is a formula (D) or (E):
  • R 3 , R 4 . R 7 and R 8 which may be the same or different, are R b . cyano, nitro, halogen. -OR b , -SR b or optionally substituted amino:
  • R5 and R ⁇ which may be the same or different, are R D . cyano or nitro; or any R R 3 or R ⁇ group, together with the interconnecting atoms, can form a 3-, 4-. 5- or 6-membered ring with any R 2 . R 4 or R 6 or any R 1 , R 2 . R 3 . R 4 , R 5 or R 6 group, together with the interconnecting atoms can form a 5- or 6-membered ring with A 2 ;
  • Rl and R 2 , or R 7 and R 8 together with the interconnecting atoms, may form a 3-, 4-, 5- or 6-membered ring, which may be substituted;
  • R D is alkyl. alkenyl, alkynyl. carbocyclyl or heterocyclyl, each of which may be substituted, or hydrogen or acyl;
  • X is oxygen or sulfur;
  • ⁇ l is oxygen, sulfur or-N(R 9 )-;
  • R 9 is R b , cyano or nitro, or R 9 and A 3 , R 1 , R 2 , R 7 or R 8 , together with the interconnecting atoms, may form a 3-, 4-, 5- or 6-membered ring, which may be substituted.
  • the 2-pyridyl group is substituted at the 3 and/or 5 position.
  • a 2 is optionally substituted phenyl, optionally substituted heterocyclyl, optionally substituted cyclohexyl or optionally substituted cyclopropyl; or
  • a J is optionally substituted phenyl, optionally substituted heterocyclyl or acyl; or [0021] R 1 . R 2 , R 3 , R 4 , R 7 and R 8 are hydrogen, optionally substituted alkyl, optionally substituted phenyl. cyano, acyl or halogen (more preferably R* and R 2 are hydrogen); or
  • R5 and R6 are hydrogen, optionally substituted alkyl or acyl; or
  • R 7 and R 8 are hydrogen, optionally substituted alkyl or acyl; or R 9 is hydrogen or optionally substituted alkyl; or the 2-pyridyl group (A ⁇ ) is substituted by alkoxy, alkyl, cyano, halogen, nitro, alkoxycarbonyl, alkylsulfmyl, alkylsulfonyl or trifluoromethyl, (preferably chlorine or trifluoromethyl).
  • Y is -L-A 2 - and:
  • a 2 is phenyl optionally substituted by halogen, haloalkyl, phenoxy, alkoxy. alkyl, CN, NO?, S0 2 -(N-tetrahydropyridinyl), alkylthio, acyl, phenylsulphonyl, dialkylamino, alkylsulphonyl, benzylsulphonyl, S(phenyl substituted by halogen): or A 2 is cycloalkyl; or naphthyl optionally substituted by NO 2 ; or
  • R 3 is hydrogen, alkyl, phenyl, halogen or acyloxy;
  • a 2 is phenyl optionally substituted by halogen, NO? or alkoxy; or thienyl; or imidazolyl; or pyrrolinyl substituted by alkoxy; or
  • L is -CH(R 3 )N(R 5 )CH 2 -;
  • R 3 is N-alkylcarbamoyl or alkoxycarbonyl; R 3 is hydrogen or acyl;
  • a 2 is phenyl optionally substituted by alkyl, alkoxy. halogen. NO?, haloalkyl or phenoxy; or is naphthyl; or
  • R J is N-alkylcarbamoyl or alkoxycarbonyl
  • a 2 is phenyl optionally substituted by alkoxy, halogen, NO?, haloalkyl, phenoxy or phenyl; or is cycloalkyl; or
  • Y is -Ll-A 3 - and:
  • R! is hydrogen
  • R 2 is hydrogen or alkoxycarbonyl
  • R! is hydrogen
  • R 2 is hydrogen or alkyl
  • R 8 and R 9 are each hydrogen or alkyl;
  • a 3 is benzoyl optionally substituted by alkyl; or benzyloxycarbonyl; or alkoxycarbonyl; or
  • R! and R 2 are each hydrogen;
  • a J is phenyl; or
  • the invention also includes any of the compounds specifically exemplified hereinafter.
  • Any alkyl group may be straight or branched and is preferably of 1 to 10 carbon atoms, especially 1 to 7 and particularly 1 to 5 carbon atoms.
  • Any alkenyl or alkynyl group may be straight or branched and is preferably of 2 to 7 carbon atoms and may contain up to 3 double or triple bonds which may be conjugated, for example vinyl, allyl. butadienyl or propargyl.
  • Any carbocyclyl group may be saturated, unsaturated or aromatic, and contain 3 to 8 ring-atoms.
  • Preferred saturated carbocyclyl groups are cyclopropyl, cyclopentyl or cyclohexyl.
  • Preferred unsaturated carbocyclyl groups contain up to 3 double bonds.
  • a preferred aromatic carbocyclyl group is phenyl.
  • the term carbocylic should be similarly construed.
  • carbocyclyl includes any fused combination of carbocyclyl groups, for example naphthyl, phenanthryl. indanyl and indenyl.
  • Any heterocyclyl group may be saturated, unsaturated or aromatic, and contain 5 to 7 ring-atoms up to 4 of which may be hetero-atoms such as nitrogen. oxygen and sulfur.
  • heterocyclyl groups are furyl, thienyl, pyrrolyl. pyrrolinyl, pyrrolidinyl. imidazolvl, dioxolanyl, oxazolyl. thiazolyl. imidazolvl. imidazolinyl. imidazolidinyl. pyrazolyl. pyrazolinyl, pyrazolidinyl. isoxazolyl, isothiazolyl, oxadiazolyl.
  • heterocyclyl includes fused heterocyclyl groups, for example benzimidazolyl, benzoxazolyl, imidazopyridinyl, benzoxazinyl. benzothiazinyl, oxazolopyridinyl, benzofuranyl, quinolinyl, quinazolinyl, quinoxalinyl, dihydroquinazolinyl, benzothiazolyl, phthalimido. benzofuranyl, benzodiazepinyl, indolyl and isoindolyl.
  • heterocyclic should be similarly construed.
  • Any alkyl, alkenyl, alkynyl, carbocyclyl or heterocyclyl group, when substituted, may be substituted by one or more substituents. which may be the same or different, and may be selected from the list: hydroxy; mercapto; azido; nitro; halogen; cyano; acyl; optionally substituted amino; optionally substituted carbocyclyl; optionally substituted heterocyclyl; cyanato: thiocyanato: -SF5; -OR a ; -
  • R a is alkyl, alkenyl, alkynyl, carbocyclyl or heterocyclyl, each of which may be substituted.
  • R a is alkyl, alkenyl, alkynyl, carbocyclyl or heterocyclyl, each of which may be substituted.
  • the list includes additionally: alkyl, alkenyl and alkynyl. each of which may be substituted.
  • Preferred substituents on any alkyl, alkenyl or alkynyl group are alkoxy, haloalkoxy or alkylthio, each containing 1 to 5 carbon atoms; halogen; or optionally substituted phenyl.
  • Preferred substituents on any carbocyclyl or heterocyclyl group are alkyl, haloalkyl, alkoxy, haloalkoxy or alkylthio. each containing 1 to 5 carbon atoms; halogen; or optionally substituted phenyl.
  • any alkyl group or any unsaturated ring-carbon in any carbocyclyl or heterocyclyl group includes a divalent group such as oxo or imino, which may be substituted by optionally substituted amino.
  • R a or -OR a Preferred groups are oxo. imino. alkylimino. oximino, alkyloximino or hydrazono.
  • Any amino group, when substituted and where appropriate, may be substituted by one or two substituents which may be the same or different, selected from the list: optionally substituted alkyl. optionally substituted amino, -OR a and acyl groups.
  • heterocyclyl group preferably a 5 to 7-membered heterocyclyl group, which may be substituted and may contain other hetero atoms, for example morpholino, thiomorpholino or piperidinyl.
  • R d is alkyl, C ⁇ to C5 alkoxy, C ⁇ to C5 alkylthio, phenyl, heterocyclyl or amino, each of which may be substituted.
  • salts salts the cations or anions of which are known and accepted in the art for the formation of salts for agricultural or horticultural use.
  • Suitable salts with bases include alkali metal (e.g. sodium and potassium), alkaline earth metal (e.g. calcium and magnesium), ammonium and amine (e.g. diethanolamine, triethanolamine. octylamine, morpholine and dioctylmethylamine) salts.
  • Suitable acid addition salts e.g. formed by compounds of formula I containing an amino group, include salts with inorganic acids, for example hydrochlorides, sulphates, phosphates and nitrates and salts with organic acids for example acetic acid.
  • Complexes of compounds of the invention are usually formed from a salt of formula MAn 2 , in which M is a divalent metal cation, e.g. copper, manganese, cobalt, nickel, iron or zinc and An is an anion, e.g. chloride, nitrate or sulfate.
  • M is a divalent metal cation, e.g. copper, manganese, cobalt, nickel, iron or zinc
  • An is an anion, e.g. chloride, nitrate or sulfate.
  • the invention includes individual isomers as well as mixtures thereof.
  • the invention includes individual isomers as l o well as mixtures thereof.
  • the compounds of the invention have activity as fungicides, especially against fungal diseases of plants, e.g. mildews and particularly cereal powdery mildew (Erysiphe graminis) and vine downy mildew (Plasmopara viticola), rice
  • the invention thus also provides a method of combating fungal pests such as phytopathogenic fungi at a locus infested or liable to be infested therewith, which 5 comprises applying to the locus a compound of formula I or a complex or salt thereof.
  • the invention also provides an agricultural composition comprising a compound of formula I or a complex or salt thereof in admixture with an 0 agriculturally acceptable diluent or carrier.
  • the composition of the invention may of course include more than one compound of the invention.
  • composition can comprise one or more additional active ingredients, for example compounds known to possess plant-growth regulant, herbicidal, fungicidal. insecticidal, acaricidal, antimicrobial or antibacterial properties.
  • additional active ingredients for example compounds known to possess plant-growth regulant, herbicidal, fungicidal. insecticidal, acaricidal, antimicrobial or antibacterial properties.
  • the compound of the invention can be used in sequence with the other active ingredient.
  • the diluent or carrier in the composition of the invention can be a solid or a liquid optionally in association with a surface-active agent, for example a dispersing agent, emulsifying agent or wetting agent.
  • Suitable surface-active agents include anionic compounds such as a carboxylate, for example a metal carboxylate of a long chain fatty acid; an N-acylsarcosinate: mono- or di-esters of phosphoric acid with fatty alcohol ethoxylates or alkyl phenol ethoxylates or salts of such esters; fatty alcohol sulfates such as sodium dodecyl sulfate, sodium octadecyl sulfate or sodium cetyl sulfate; ethoxylated fatty alcohol sulfates; ethoxylated alkylphenol sulfates; lignin sulfonates; petroleum sulfonates; alkyl-aryl sulf
  • butyl-naphthalene sulfonate salts of sulfonated naphthalene-formaldehyde condensates: salts of sulfonated phenol-formaldehyde condensates; or more complex sulfonates such as the amide sulfonates, e.g. the sulfonated condensation product of oleic acid and N-methyl taurine; the dialkyl sulfosuccinates. e.g. the sodium sulfonate of dioctyl succinate; acid derivatives of alkyl glycosides and alkylpolyglycosides materials and their metal salts, e.g. alkyl polyglycoside citrate or tartrate materials: or mono-, di- and tri-alkyl esters of citric acid and their metal salts.
  • the amide sulfonates e.g. the sulfonated condensation product of oleic acid and
  • ⁇ onionic agents include condensation products of fatty acid esters, fatty alcohols, fatty acid amides or fatty-alkyl- or alkenyl-substituted phenols with ethylene and/or propylene oxide; fatty esters of polyhydric alcohol ethers, e.g. sorbitan fatty acid esters; condensation products of such esters with ethylene oxide, e.g. polyoxyethylene sorbitan fatty acid esters; alkyl glycosides.
  • alkyl polyglycoside materials block copolymers of ethylene oxide and propylene oxide; acetylenic glycols such as 2,4,7,9-tetramethyl-5-decyne-4,7-diol, ethoxylated acetylenic glycols; acrylic based graft copolymers; alkoxylated siloxane surfactants; or imidazoline type surfactants, e.g. l-hydroxyethyl-2-alkylimidazoline.
  • Examples of a cationic surface-active agent include, for instance, an aliphatic mono-, di-, or polyamine as an acetate, naphthenate or oleate; an oxygen-containing amine such as an amine oxide, polyoxyethylene alkylamine or polyoxypropylene alkylamine; an amide-linked amine prepared by the condensation of a carboxylic acid with a di- or polyamine: or a quaternary ammonium salt.
  • compositions of the invention can take any form known in the art for the formulation of agrochemicals, for example, a solution, an aerosol, a dispersion, an aqueous emulsion, a microemulsion, a dispersible concentrate, a dusting powder, a seed dressing, a fumigant, a smoke, a dispersible powder, an emulsifiable concentrate, granules or an impregnated strip.
  • a dispersible concentrate comprises a compound of the invention dissolved in one or more water miscible or semi-water miscible solvents together with one or more surface active and/or polymeric material. Addition of the formulation to water results in the crystallisation of the active ingredient, the process being controlled by the surfactants and/or polymers resulting in a fine dispersion.
  • a dusting powder comprises a compound of the invention intimately mixed and ground with a solid pulverulent diluent, for example, kaolin.
  • An emulsifiable concentrate comprises a compound of the invention dissolved in a water-immiscible solvent which forms an emulsion or microemulsion on addition to water in the presence of an emulsifying agent.
  • a granular solid comprises a compound of the invention associated with similar diluents to those that may be employed in dusting powders, but the mixture is granulated by known methods. Alternatively it comprises the active ingredient absorbed or coated on a pre-formed granular carrier, for example, Fuller's earth, attapulgite, silica or limestone grit.
  • Wettable powders, granules or grains usually comprise the active ingredient in admixture with suitable surfactants and an inert powder diluent such as clay or diatomaceous earth.
  • Another suitable concentrate is a flowable suspension concentrate which is formed by grinding the compound with water or other liquid, surfactants and a suspending agent.
  • the concentration of the active ingredient in the composition of the present invention, as applied to plants is preferably within the range of 0.0001 to 1.0 per cent by weight, especially 0.0001 to 0.01 per cent by weight.
  • the amount of active ingredient can vary widely and can be, for example, from 5 to 95 per cent by weight of the composition.
  • the invention is generally applied to seeds, plants or their habitat.
  • the compound can be applied directly to the soil before, at or after drilling so that the presence of active compound in the soil can control the growth of fungi which may attack seeds.
  • the active compound can be applied in any manner which allows it to be intimately mixed with the soil such as by spraying, by broadcasting a solid form of granules, or by applying the active ingredient at the same time as drilling by inserting it in the same drill as the seeds.
  • a suitable application rate is within the range of from 5 to 1000 g per hectare, more preferably from 10 to 500 g per hectare.
  • the active compound can be applied directly to the plant by, for example, spraying or dusting either at the time when the fungus has begun to appear on the plant or before the appearance of fungus as a protective measure.
  • the preferred mode of application is by foliar spraying. It is generally important to obtain good control of fungi in the early stages of plant growth, as this is the time when the plant can be most severely damaged.
  • the spray or dust can conveniently contain a pre- or post-emergence herbicide if this is thought necessary.
  • a suitable rate of application is from 0.025 to 5 kg per hectare, preferably from 0.05 to 1 kg per hectare.
  • the compounds of the invention can be applied to harvested fruits, vegetables or seeds to prevent infection during storage.
  • the compounds of the invention can be applied to plants or parts thereof which have been genetically modified to exhibit a trait such as fungal and/or herbicidal resistance.
  • the compounds of the invention can be used to treat fungal infestations in timber and in public health applications.
  • Compounds of the invention may be prepared, in known manner, in a variety of ways. Such processes for the preparation of novel compounds of formula I constitute a feature of the invention.
  • preferred base is triethylamine
  • Collections of compounds of formula (I) may also be prepared in a parallel manner, either manually, automatically or semi-automaticalh This parallel preparation may be applied to the reaction procedure, work-up or purification of products or intermediates
  • This parallel preparation may be applied to the reaction procedure, work-up or purification of products or intermediates
  • compounds of the formula (I) may be prepared using so d- supported methods, where the reactants are bound to a synthetic resin See for example Barry A Bunin in 'The Combinatorial Index " '. Academic Press. 1998 and ' The tea-bag method " (Houghten. US 4.631. 1 1 : Houghten et al.. Proc. Natl. Acad. Sci. 1985. 82. 5131 -5135).
  • Compounds of formula Va may be prepared by treating XV with a compound of formula XVI in the presence of a suitable base, such as triethylamine.
  • Compounds of formula Vb may be prepared from compounds of formula XVa by treatment with compounds of formula XVII. sodium cvanoborohvdnde and acetic acid followed by reaction with compounds of formula XVIII and triethylamine.
  • Intermediates of formula XI may be prepared according to Scheme 13 by reacting compounds of formula VIII in the presence of a suitable base such as triethylamine with compounds of formula XIX. in the presence of a carbonyl diimidazole (CDI).
  • a suitable base such as triethylamine
  • CDI carbonyl diimidazole
  • R z are hv drogen and L is -CH(R , )N(R- ) )CH -.
  • the resulting white solid was isolated by filtration, washed with water, redissolved in ethyl acetate and the organic solution dried and evaporated to yield the intermediate phthalimide as a white solid.
  • the phthalimide (2.0 g) was dissolved in methanol (20 ml) and the resulting solution treated with hydrazine hydrate (0.42 g). The reaction was left to stand for 19 hours before heating at reflux for 3 hours to yield a white precipitate.
  • the reaction mixture was filtered and the methanol filtrate evaporated. The residue was treated with diethyl ether and refiltered. Evaporation of the filtrate yielded the title compound as a green vellow oil.
  • Compounds were assessed for activity against one or more of the following.
  • Phytophthora infestans late tomato blight Plasmopara viticola- vine downy mildew Erysiphe grammisf sp triticv. wheat powdery mildew Pyricularia oryzae: rice blast Leptosphaeria nodorum- glume blotch
  • Aqueous solutions or dispersions of the compounds at the desired concentration, including a wetting agent, were applied by spray or by drenching the stem base of the test plants, as appropriate.
  • plants or plant parts were inoculated with appropriate test pathogens before or after application of the compounds as appropriate, and kept under controlled environmental conditions suitable for maintaining plant growth and development of the disease.
  • the degree of infection of the affected part of the plant was visuallv estimated Compounds are assessed on a score of 1 to 3 where 1 is little or no control. 2 is moderate control and 3 is good to total control At a concentration of 500 ppm (w/v) or less, the following compounds scored 2 or more against the fungi specified.
  • Plasmopara viticola 50. 55. 104. 105. 201. 21 " $. 221. 222. 224. 225.
  • Levto vhaeria nodorum 13. 105. 107. 108. 201. 229. 232. 238. 317. 336 and 626.

Abstract

L'invention a trait à des composés représentés par la formule générale (I), dans laquelle A?1, R1, R2¿ et Y sont tels que définis dans la description; et à leur utilisation comme fongicides phytopathogènes.
PCT/EP2000/008143 1999-08-18 2000-08-09 Fongicides WO2001011965A1 (fr)

Priority Applications (8)

Application Number Priority Date Filing Date Title
JP2001516328A JP4936623B2 (ja) 1999-08-18 2000-08-09 殺菌剤
AT00960499T ATE270817T1 (de) 1999-08-18 2000-08-09 Fungizide
MXPA02001453A MXPA02001453A (es) 1999-08-18 2000-08-09 Fungicidas.
BR0013371-0A BR0013371A (pt) 1999-08-18 2000-08-09 Uso de um composto, métodos de combate de pestes fúngicas e de fungos fitopatogênicos, composições pesticida e fungicida, e, composto
US10/049,976 US6821992B1 (en) 1999-08-18 2000-08-09 Fungicides
DE60012188T DE60012188T2 (de) 1999-08-18 2000-08-09 Fungizide
AU72785/00A AU7278500A (en) 1999-08-18 2000-08-09 Fungicides
EP00960499A EP1204323B1 (fr) 1999-08-18 2000-08-09 Fongicides

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
GB9919500.0 1999-08-18
GBGB9919499.5A GB9919499D0 (en) 1999-08-18 1999-08-18 Fungicidal compounds
GBGB9919500.0A GB9919500D0 (en) 1999-08-18 1999-08-18 Fungicidal compounds
GB9919499.5 1999-08-18

Publications (1)

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WO2001011965A1 true WO2001011965A1 (fr) 2001-02-22

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PCT/EP2000/008143 WO2001011965A1 (fr) 1999-08-18 2000-08-09 Fongicides

Country Status (13)

Country Link
US (1) US6821992B1 (fr)
EP (1) EP1204323B1 (fr)
JP (1) JP4936623B2 (fr)
KR (1) KR100718863B1 (fr)
CN (1) CN1209016C (fr)
AT (1) ATE270817T1 (fr)
AU (1) AU7278500A (fr)
BR (1) BR0013371A (fr)
DE (1) DE60012188T2 (fr)
ES (1) ES2220533T3 (fr)
MX (1) MXPA02001453A (fr)
PT (1) PT1204323E (fr)
WO (1) WO2001011965A1 (fr)

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US7074742B2 (en) 2000-09-18 2006-07-11 E. I. Du Pont De Nemours And Company Pyridinyl amides and imides for use as fungicides
JP2005535714A (ja) * 2002-08-12 2005-11-24 バイエル・クロツプサイエンス・エス・アー 新規２−ピリジルエチルベンズアミド誘導体
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WO2005077179A1 (fr) * 2004-02-12 2005-08-25 Bayer Cropscience Sa Composition fongique comprenant un derive de pyridylethylbenzamide et un compose capable d'inhiber la biosynthese de la melanine
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WO2005077180A1 (fr) * 2004-02-12 2005-08-25 Bayer Cropscience Sa Composition fongique comprenant un derive de pyridylethylbenzamide et un compose capable d'inhiber la mitose et la division cellulaire
JP4685035B2 (ja) * 2004-02-12 2011-05-18 バイエル・クロツプサイエンス・アクチエンゲゼルシヤフト ピリジルエチルベンズアミド誘導体及びエルゴステロール生合成を阻害することが可能な化合物を含んでいる殺菌剤組成物
WO2005077183A1 (fr) * 2004-02-12 2005-08-25 Bayer Cropscience Sa Composition fongicide contenant un derive de pyridylethylbenzamide et un compose capable d'inhiber la biosynthese des sterols
AU2005213186B2 (en) * 2004-02-12 2010-10-14 Bayer Cropscience Aktiengesellschaft Fungicidal composition comprising a pyridylethylbenzamide derivative and a compound capable of inhibiting the ergosterol biosynthesis
AU2005213184B2 (en) * 2004-02-12 2010-10-14 Bayer Cropscience Aktiengesellschaft Fungicidal composition comprising a pyridylethylbenzamide derivative and a compound capable of inhibiting the spores germination or mycelium growth by acting on different metabolic routes
JP2007522186A (ja) * 2004-02-12 2007-08-09 バイエル・クロツプサイエンス・エス・アー ピリジルエチルベンズアミド誘導体及びメチオニン生合成を阻害することが可能な化合物を含んでいる殺菌剤組成物
JP2007522187A (ja) * 2004-02-12 2007-08-09 バイエル・クロツプサイエンス・エス・アー ピリジルエチルベンズアミド誘導体及びエルゴステロール生合成を阻害することが可能な化合物を含んでいる殺菌剤組成物
AU2005212839B2 (en) * 2004-02-12 2010-09-16 Bayer Cropscience Aktiengesellschaft Fungicidal composition comprising a pyridylethylbenzamide derivative and a compound capable of inhibiting the transport of electrons of the respiratory chain in phytopathogenic fungal organisms
US7786148B2 (en) 2004-02-12 2010-08-31 Bayer Cropscience S.A. Fungicidal composition comprising a pyridylethylbenzamide derivative and a compound capable of inhibiting the transport of electrons of the respiratory chain in phytopathogenic fungal organisms
US7776892B2 (en) 2004-02-12 2010-08-17 Bayer Cropscience S.A. Fungicidal composition comprising a pyridylethylbenzamide derivative and a compound capable of inhibiting the spores germination or mycelium growth by acting on different metabolic routes
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AU7278500A (en) 2001-03-13
MXPA02001453A (es) 2003-01-28
DE60012188D1 (de) 2004-08-19
KR100718863B1 (ko) 2007-05-16
CN1209016C (zh) 2005-07-06
EP1204323B1 (fr) 2004-07-14
DE60012188T2 (de) 2005-08-25
JP2003506465A (ja) 2003-02-18
ES2220533T3 (es) 2004-12-16
KR20020059365A (ko) 2002-07-12
JP4936623B2 (ja) 2012-05-23
US6821992B1 (en) 2004-11-23
ATE270817T1 (de) 2004-07-15
EP1204323A1 (fr) 2002-05-15
CN1370047A (zh) 2002-09-18
BR0013371A (pt) 2002-05-07
PT1204323E (pt) 2004-11-30

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